Two different clinical phenotypes of Creutzfeldt-Jakob disease with a M232R substitution

Classification of sporadic Creutzfeldt-Jakob disease based on molecular and phenotypic analysis of 300 subjects

Piero Parchi, Armin Giese, Sabina Capellari et al. · Annals of Neurology · 1999 · 1.4K citations

Veterinary Medicine, Genetics, Neurology +17

Fatal Familial Insomnia and Familial Creutzfeldt-Jakob Disease: Disease Phenotype Determined by a DNA Polymorphism

Lev G. Goldfarb, Robert B. Petersen, Massimo Tabaton et al. · Science · 1992 · 718 citations

Life Sciences, Genetics, Molecular Genetics +17

Genetic prion disease: the EUROCJD experience

Gábor G. Kovács, Maria Puopolo, Anna Ladogana et al. · Human Genetics · 2005 · 448 citations

Veterinary Medicine, Genetics, Infectious Diseases +14

Molecular classification of sporadic Creutzfeldt–Jakob disease

Andrew F. Hill, Susan Joiner, Jonathan D. F. Wadsworth et al. · Brain · 2003 · 377 citations

Veterinary Medicine, Molecular Biology, Neurology +15

Fatal familial insomnia and familial Creutzfeldt-Jakob disease: different prion proteins determined by a DNA polymorphism.

L. Monari, Shu G. Chen, Patrick O. Brown et al. · Proceedings of the National Academy of Sciences · 1994 · 332 citations · Full text

Veterinary Medicine, Genetics, Molecular Genetics +17